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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00152737
Other study ID # PHRC 03-01
Secondary ID
Status Completed
Phase N/A
First received September 8, 2005
Last updated July 16, 2015
Start date March 2004
Est. completion date July 2008

Study information

Verified date July 2015
Source University Hospital, Angers
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

The whole study is divided in 4 parallel protocols. The first protocol estimates the reliability of the technique through test-retest recordings. The second protocol aims to prove that exercise Tcpo2 is efficient to estimate the benefit of proximal revascularisation on proximal and distal ischemia in patients suffering stage two lower extremity arterial disease. The third protocol aims at estimating with exercise tcpo2 the eventual apparison of proximal ischemia after aorto-bi-femoral bypasses. The last protocol is a transversal study of patients with aorto-bi-femoral bypasses aiming to analyse the presence of proximal and distal symptoms and ischemia.

The hypothesis for protocol 2 is that TcpO2 at exercise is significantly improved after surgery at the aortic and primary iliac artery. The hypothesis for protocols 3 and 4 relates on the hypothesis that a significant number of patients benefiting aorto-bi-femoral bypass suffer isolated proximal pain/ischemia after surgery.

Amendement to the project has been recently validated to study the neurologic and bone complication of chronic vascular ischemia


Description:

Patients included are submitted to:

San Diego Claudication Questionnaire before and during the treadmill test Treadmill test(s) through the Strandness procedure (2MPh 10% slope) Transcutaneous oxygen pressure recording before during and after exercise Ankle and brachial pressure measurements. Neurologic investigation with Quantitative sensory Testing (QST) and neurophysiological tests for patients included in the sub-group analysing neurologic complication Whole body densitometry for patients included in the sub-group analysing osteo-articular complications


Recruitment information / eligibility

Status Completed
Enrollment 165
Est. completion date July 2008
Est. primary completion date July 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- protocol 1 - 3 stage 2 claudication

- Protocols 2 & 3 : Indication for surgery

- protocol 4 : Patent aorto bio femoral bypass for more than 4 months

- Ability to perform a treadmill test

Exclusion Criteria:

- Stage 4 LEAD

- Aortic aneurysm

- Acute coronary syndrom

- claudication of documented non vascular origin (for protocols 1-3 only)

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Procedure:
Exercise test with Transcutaneous oxygene pressure
Ce marked devices
Ankle and arm pressure values
one test before and one test after surgery

Locations

Country Name City State
France Laboratoire d'explorations vasculaires Angers

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Angers Sanofi-Synthelabo, Société Française de Médecine Vasculaire

Country where clinical trial is conducted

France, 

References & Publications (2)

Jaquinandi V, Abraham P, Picquet J, Paisant-Thouveny F, Leftheriotis G, Saumet JL. Estimation of the functional role of arterial pathways to the buttock circulation during treadmill walking in patients with claudication. J Appl Physiol (1985). 2007 Mar;10 — View Citation

Jaquinandi V, Picquet J, Bouyé P, Saumet JL, Leftheriotis G, Abraham P. High prevalence of proximal claudication among patients with patent aortobifemoral bypasses. J Vasc Surg. 2007 Feb;45(2):312-8. — View Citation

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